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. 2020 Jul 30;18(7):e3000562. doi: 10.1371/journal.pbio.3000562

Fig 3. Characterization of viral dynamics of HCV JFH-1 and Jc1-n.

Fig 3

The distributions of the rate constant for infection, βθ; the release rate of intracellular viral RNA, ρ; the converted fraction of infectious viral RNA, fθ; and the replication rate of intracellular viral RNA, k, inferred by MCMC computations are shown in (A), (B), (C) and (D), respectively, for HCV JFH-1 (orange) and Jc1-n (green). Parameters βθ and ρ for Jc1-n were significantly larger than for JFH-1, whereas there was no significant difference in fθ between the two strains as assessed by repeated bootstrap t test. JFH-1 and Jc1-n stains had identical viral RNA replication rates. The distributions of accumulation rates of intracellular viral RNA, kμρ, and the Malthusian parameter, M, calculated from all accepted MCMC parameter estimates are shown in (E) and (F), respectively, for HCV JFH-1 (orange) and Jc1-n (green). These indices were significantly larger for JFH-1 than for Jc1-n as assessed by the repeated bootstrap t test. The underlying data for this Figure can be found in S2 Data. HCV, hepatitis C virus; MCMC, Markov chain Monte Carlo.